Severe Cleidocranial dysplasia and Hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2

Por El-Gharbawy, Areeg H., Peeden, Joseph N., Lachman, Ralph S., Graham, John M., Moore, Stephen R., Rimoin, David L.
Publicado em 2010

Genomic instability after targeted irradiation of human lymphocytes: Evidence for inter-individual differences under bystander conditions

Por Kadhim, Munira A., Lee, Ryonfa, Moore, Stephen R., Macdonald, Denise A., Chapman, Kim L., Patel, Gaurang, Prise, Kevin M.
Publicado em 2010

Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells

Por Akagi, Tadayuki, Shih, Lee-Yung, Ogawa, Seishi, Gerss, Joachim, Moore, Stephen R., Schreck, Rhona, Kawamata, Norihiko, Liang, Der-Cherng, Sanada, Masashi, Nannya, Yasuhito, Deneberg, Stefan, Zachariadis, Vasilios, Nordgren, Ann, Song, Jee Hoon, Dugas, Martin, Lehmann, Sören, Koeffler, H. Phillip
Publicado em 2009